Takeshi Rikiishi

GNE myopathy associated with congenital thrombocytopenia: A report of two siblings

Rumiko Izumi, Tetsuya Niihori, Naoki Suzuki et al. · Neuromuscular Disorders · 2014 · 71 citations

Gne Myopathy, Congenital Thrombocytopenia, Pediatrics +1

Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

Shoko Komatsuzaki, Yoko Aoki, Tetsuya Niihori et al. · Journal of Human Genetics · 2010 · 57 citations · Full text

Noonan-like Syndrome, Mendelian Disorder, Genetic Disorder +6

Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation

Kunihiko Moriya, Tasuku Suzuki, Nao Uchida et al. · International Journal of Hematology · 2020 · 32 citations

Rheumatology, Autoimmune Disease, Ruxolitinib Treatment +7

Somatic BRAF c.1799T>A p.V600E Mosaicism syndrome characterized by a linear syringocystadenoma papilliferum, anaplastic astrocytoma, and ocular abnormalities

Yuko Watanabe, Kosuke Shido, Tetsuya Niihori et al. · American Journal of Medical Genetics Part A · 2015 · 27 citations

Hypercalcemia due to all‐<i>trans</i> retinoic acid therapy for acute promyelocytic leukemia: A case report of effective treatment with bisphosphonate

Osamu Sakamoto, Miyako Yoshinari, Takeshi Rikiishi et al. · Pediatrics International · 2001 · 26 citations

Radiation Oncology, Acute Promyelocytic Leukemia, Effective Treatment +1